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Photophysical properties of CdSe quantum dot self-assemblies with zinc phthalocyanines and azaphthalocyanines

The formation of self-assemblies between CdSe quantum dots (QDs) and Zn phthalocyanines (Pc) and azaphthalocyanines (AzaPc) bearing alkylsulfanyl substituents and the photophysical properties of these assemblies were studied using both steady-state and time-resolved luminescence/absorption spectrosc...

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Published in:Photochemical & photobiological sciences 2013-05, Vol.12 (5), p.743-75
Main Authors: Suchánek, Jan, Lang, Kamil, Novakova, Veronika, Zimcik, Petr, Zelinger, Zden k, Kubát, Pavel
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description The formation of self-assemblies between CdSe quantum dots (QDs) and Zn phthalocyanines (Pc) and azaphthalocyanines (AzaPc) bearing alkylsulfanyl substituents and the photophysical properties of these assemblies were studied using both steady-state and time-resolved luminescence/absorption spectroscopy. The formation of the self-assemblies was accompanied by a blue shift of the Q band of the dyes and by a quenching of the CdSe QDs luminescence. The largest spectral shift of the Q-band was approximately 7 nm and was observed for pentan-3-ylsulfanyl-functionalised phthalocyanine ( 3 ). Assuming a 1 : 1 stoichiometry, the calculated binding constant was 4 × 10 4 M −1 . Pc substituted with the bulky tert -butylsulfanyl groups ( 1 ) exhibited a smaller shift of the Q band. The quenching of the CdSe QDs luminescence by 1 was more effective than that observed for 3 . The results indicated that the luminescence quenching may be due to a photoinduced charge transfer between 1 or 3 and the CdSe QDs. In contrast, the AzaPc ( 2 ) with the same substituents as 1 had little effect on the QDs luminescence. For all cases, we found an inefficient resonance energy transfer between the attached dyes and the CdSe QD. The formation of the self-assemblies had negligible effects on the photogeneration of the singlet oxygen, O 2 ( 1 Δ g ), that was fully controlled only by the absorption of the light by the macrocycles. The formation and the photophysical properties of self-assemblies between CdSe quantum dots and Zn phthalocyanines and azaphthalocyanines bearing alkylsulfanyl substituents were studied using luminescence/absorption spectroscopy.
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The formation of the self-assemblies was accompanied by a blue shift of the Q band of the dyes and by a quenching of the CdSe QDs luminescence. The largest spectral shift of the Q-band was approximately 7 nm and was observed for pentan-3-ylsulfanyl-functionalised phthalocyanine ( 3 ). Assuming a 1 : 1 stoichiometry, the calculated binding constant was 4 × 10 4 M −1 . Pc substituted with the bulky tert -butylsulfanyl groups ( 1 ) exhibited a smaller shift of the Q band. The quenching of the CdSe QDs luminescence by 1 was more effective than that observed for 3 . The results indicated that the luminescence quenching may be due to a photoinduced charge transfer between 1 or 3 and the CdSe QDs. In contrast, the AzaPc ( 2 ) with the same substituents as 1 had little effect on the QDs luminescence. For all cases, we found an inefficient resonance energy transfer between the attached dyes and the CdSe QD. The formation of the self-assemblies had negligible effects on the photogeneration of the singlet oxygen, O 2 ( 1 Δ g ), that was fully controlled only by the absorption of the light by the macrocycles. The formation and the photophysical properties of self-assemblies between CdSe quantum dots and Zn phthalocyanines and azaphthalocyanines bearing alkylsulfanyl substituents were studied using luminescence/absorption spectroscopy.</description><identifier>ISSN: 1474-905X</identifier><identifier>EISSN: 1474-9092</identifier><identifier>DOI: 10.1039/c2pp25348h</identifier><identifier>PMID: 23318549</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>Biochemistry ; Biomaterials ; Cadmium Compounds - chemistry ; Chemistry ; Indoles - chemistry ; Organometallic Compounds - chemistry ; Particle Size ; Physical Chemistry ; Plant Sciences ; Quantum Dots ; Quantum Theory ; Selenium Compounds - chemistry ; Solvents - chemistry ; Spectrometry, Fluorescence</subject><ispartof>Photochemical &amp; photobiological sciences, 2013-05, Vol.12 (5), p.743-75</ispartof><rights>The Royal Society of Chemistry and Owner Societies 2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c407t-9c2a89f1a375872ad5da3d249beca36ebf85a389250a182950683a9a0ab6b9ec3</citedby><cites>FETCH-LOGICAL-c407t-9c2a89f1a375872ad5da3d249beca36ebf85a389250a182950683a9a0ab6b9ec3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23318549$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Suchánek, Jan</creatorcontrib><creatorcontrib>Lang, Kamil</creatorcontrib><creatorcontrib>Novakova, Veronika</creatorcontrib><creatorcontrib>Zimcik, Petr</creatorcontrib><creatorcontrib>Zelinger, Zden k</creatorcontrib><creatorcontrib>Kubát, Pavel</creatorcontrib><title>Photophysical properties of CdSe quantum dot self-assemblies with zinc phthalocyanines and azaphthalocyanines</title><title>Photochemical &amp; photobiological sciences</title><addtitle>Photochem Photobiol Sci</addtitle><addtitle>Photochem Photobiol Sci</addtitle><description>The formation of self-assemblies between CdSe quantum dots (QDs) and Zn phthalocyanines (Pc) and azaphthalocyanines (AzaPc) bearing alkylsulfanyl substituents and the photophysical properties of these assemblies were studied using both steady-state and time-resolved luminescence/absorption spectroscopy. The formation of the self-assemblies was accompanied by a blue shift of the Q band of the dyes and by a quenching of the CdSe QDs luminescence. The largest spectral shift of the Q-band was approximately 7 nm and was observed for pentan-3-ylsulfanyl-functionalised phthalocyanine ( 3 ). Assuming a 1 : 1 stoichiometry, the calculated binding constant was 4 × 10 4 M −1 . Pc substituted with the bulky tert -butylsulfanyl groups ( 1 ) exhibited a smaller shift of the Q band. The quenching of the CdSe QDs luminescence by 1 was more effective than that observed for 3 . The results indicated that the luminescence quenching may be due to a photoinduced charge transfer between 1 or 3 and the CdSe QDs. In contrast, the AzaPc ( 2 ) with the same substituents as 1 had little effect on the QDs luminescence. For all cases, we found an inefficient resonance energy transfer between the attached dyes and the CdSe QD. 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The formation of the self-assemblies was accompanied by a blue shift of the Q band of the dyes and by a quenching of the CdSe QDs luminescence. The largest spectral shift of the Q-band was approximately 7 nm and was observed for pentan-3-ylsulfanyl-functionalised phthalocyanine ( 3 ). Assuming a 1 : 1 stoichiometry, the calculated binding constant was 4 × 10 4 M −1 . Pc substituted with the bulky tert -butylsulfanyl groups ( 1 ) exhibited a smaller shift of the Q band. The quenching of the CdSe QDs luminescence by 1 was more effective than that observed for 3 . The results indicated that the luminescence quenching may be due to a photoinduced charge transfer between 1 or 3 and the CdSe QDs. In contrast, the AzaPc ( 2 ) with the same substituents as 1 had little effect on the QDs luminescence. For all cases, we found an inefficient resonance energy transfer between the attached dyes and the CdSe QD. The formation of the self-assemblies had negligible effects on the photogeneration of the singlet oxygen, O 2 ( 1 Δ g ), that was fully controlled only by the absorption of the light by the macrocycles. The formation and the photophysical properties of self-assemblies between CdSe quantum dots and Zn phthalocyanines and azaphthalocyanines bearing alkylsulfanyl substituents were studied using luminescence/absorption spectroscopy.</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><pmid>23318549</pmid><doi>10.1039/c2pp25348h</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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subjects Biochemistry
Biomaterials
Cadmium Compounds - chemistry
Chemistry
Indoles - chemistry
Organometallic Compounds - chemistry
Particle Size
Physical Chemistry
Plant Sciences
Quantum Dots
Quantum Theory
Selenium Compounds - chemistry
Solvents - chemistry
Spectrometry, Fluorescence
title Photophysical properties of CdSe quantum dot self-assemblies with zinc phthalocyanines and azaphthalocyanines
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